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- 2006
-
Mark
Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies
(
- Contribution to journal › Article
- 2005
-
Mark
Classification of BRCA1 missense variants of unknown clinical significance
(
- Contribution to journal › Article
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Mark
Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies
(
- Contribution to journal › Article
-
Mark
A male-specific quantitative trait locus on 1p21 controlling human stature
(
- Contribution to journal › Article
-
Mark
Association of oestrogen receptor alpha gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of bone
(
- Contribution to journal › Article
- 2004
-
Mark
Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC
(
- Contribution to journal › Article
-
Mark
Genetic and functional evaluation of an interleukin-12 polymorphism (IDDM18) in families with type 1 diabetes
(
- Contribution to journal › Article
-
Mark
Familial renal cell cancer appears to have a recessive component
(
- Contribution to journal › Letter
- 2002
-
Mark
Genome screening of coeliac disease
(
- Contribution to journal › Article
- 2001
-
Mark
BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age
(
- Contribution to journal › Article
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